ANTICUERPOS ANTI-CENTRÓMERO B.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·BIO SIMEX, S.A. DE C.V.·Registered April 17, 2019REACTIVOS PARA LA DETERMINACIÓN CUALITATIVA Y CUANTITATIVA DE ANTICUERPOS ANTI-CENTRÓMERO B EN SUERO O PLASMA HUMANOS. AGENTE DE DIAGNÓSTICO IN VITRO Y PARA USO EXCLUSIVO EN LABORATORIO CLÍNICO O DE GABINETE.
REAGENTS FOR THE QUALITATIVE AND QUANTITATIVE DETERMINATION OF ANTI-CENTROMERE B ANTIBODIES IN HUMAN SERUM OR PLASMA. IN VITRO DIAGNOSTIC AGENT AND FOR EXCLUSIVE USE IN CLINICAL OR CABINET LABORATORY.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVOS PARA LA DETERMINACIÓN DE ANTICUERPOS ANTI-CENTRÓMERO B.
- Trade Name (English)
- REAGENTS FOR THE DETERMINATION OF ANTI-CENTROMERE B ANTIBODIES.
- Analysis ID
- 808R2019 SSA
- Registration Date
- April 17, 2019
- Name (Spanish)
- BIO SIMEX, S.A. DE C.V.
- Name (English)
- BIO SIMEX, S.A. DE C.V.
Access comprehensive regulatory information for ANTICUERPOS ANTI-CENTRÓMERO B. (ANTI-CENTROMERE B ANTIBODIES.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 808R2019 SSA and manufactured by BIO SIMEX, S.A. DE C.V.. The device was registered on April 17, 2019.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.